Efficacy and Safety of DLBS3233 in Prediabetic Patients (DIPPER-DM)
Status and phase
Conditions
Treatments
Details and patient eligibility
About
This is a 2-arm, prospective, double blind, randomized, and controlled clinical study for 12 weeks of therapy to investigate clinical efficacy and safety of DLBS3233.
It is hypothesized that DLBS3233 will delay the progress of beta-cell dysfunction as measured by the improvement of prandial (particularly the first phase) insulin secretion as well as insulin resistance in prediabetic subjects which may prevent the conversion of prediabetes into type 2 diabetes mellitus.
Full description
There will be two groups of treatment in this study who will receive DLBS3233 or placebo of DLBS3233 for 12 weeks of therapy.
Subjects will be provided with an education on lifestyle modification given by the assigned nutritionist. All subjects will be advised to follow such a lifestyle modification throughout the study period.
All subjects will be under direct supervision of a medical doctor during the study period.
All clinical and laboratory examinations to evaluate the investigational drug's efficacy, will be performed at baseline, Week 8th and Week 12th (end) of study treatment. Blood glucose level (both FPG and 2h-PG) will be performed at baseline and at interval of 4 weeks over the 12 weeks of study treatment. Safety examinations will be performed at baseline and at the end of study. Occurrence of adverse event will be observed during the study.
Enrollment
Sex
Ages
Volunteers
Inclusion criteria
- Male or female subjects with age of 18-60 years
- Prediabetic patients (2h-PPPG level of 140-199 mg/dL)
- Serum ALT ≤ 2.5 times upper limit of normal
- Serum creatinine < 1.5 times upper limit of normal
- Able to take oral medication
Exclusion criteria
- Female of childbearing potential
- History of diabetes mellitus
- History of symptomatic coronary arterial disease, stroke, and cardiovascular events
- Current treatment with systemic corticosteroids or herbal (alternative) medicines
- Any other disease state or uncontrolled illness, which judged by the investigator, could interfere with trial participation or trial evaluation
- Participation in any other clinical studies within 30 days prior to screening
Trial design
Primary purpose
Allocation
Interventional model
Masking
80 participants in 2 patient groups, including a placebo group
Trial contacts and locations
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Data sourced from clinicaltrials.gov
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